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Research Article
Maesa flabellifera (Primulaceae), a new species from southeast Yunnan, China
expand article infoDan Wei, Yuan Xu§|, Gang Hao, Timothy M. A. Utteridge
‡ South China Agricultural University, Guangzhou, China
§ South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, China
| South China National Botanical Garden, Guangzhou, China
¶ Singapore Botanic Gardens, Singapore, Singapore
Open Access

Abstract

Maesa flabellifera (Primulaceae-Maesoideae) from southeast Yunnan, China, is described and illustrated here. This new species belongs to the informal long corolla-tube species group and is morphologically similar to M. permollis and M. kurzii, but can be distinguished by lacking hairs, membranaceous leaves and long panicles with 7−16 branches. According to the IUCN criteria, M. flabellifera is assessed as “Least Concern”.

Key words

Ericales, Maesoideae, morphology, taxonomy, Yunnan

Introduction

The genus Maesa Forssk. (Primulaceae) contains approximately 185 species mainly distributed in tropical regions of the Old World from southern Africa through to the islands of the Pacific (Mez 1902; POWO 2024). It was originally placed in the monotypic subfamily Maesoideae of Myrsinaceae and later elevated to familial level as Maesaceae by Anderberg (2000). It is now included in an enlarged Primulaceae s.l. which includes four former families (Maesaceae, Myrsinaceae, Primulaceae and Theophrastaceae) and recognised as the only genus in the subfamily Maesoideae (APG 2016). According to the phylogenetic analysis, Maesa was found to form a basal branch, sister to all other Primulaceae species (Anderberg and Stähl 1995; Anderberg et al. 1998; Källersjö et al. 2000). Species of the genus Maesa are shrubs, trees or scramblers (Bremer et al. 2009) and can be distinguished from other genera of Primulaceae by the semi-inferior ovary, two bracteoles subtending each flower and black glandular lines scattered on the leaves, flowers and fruits (Sumanon et al. 2023).

Currently, approximately 35 species and two varieties (with 13 endemics) of Maesa have been recorded from China and they are mainly distributed in south-western China, especially in Yunnan Province. The first comprehensive revision of Maesa in China was conducted by Walker (1940). Chen (1979) recognised 29 species and one variety in China and divided these species into two sections, namely Maesa sect. Maesa and M. sect. Doraena [Thunb.] Nakai. Chen and Pipoly (1996) reviewed the Chinese species in the Flora of China and recognised 29 species. Recently, a few taxonomic reports of Maesa have been published from China (Yu et al 2016; Ding et al 2023).

In February 2021, during a field survey by the first author and colleagues in Dawei Mountain National Nature Reserve in Pingbian County, Honghe Prefecture, Yunnan, an unknown species of Maesa in blossom was encountered and gathered. In March 2023, the same plants were discovered again in two other counties of Honghe Prefecture, namely Yuanyang and Lüchun. After a careful comparison with similar species from China and adjacent countries, it was confirmed that this species is a distinct new one and is described here.

Materials and methods

Three field populations from Honghe Prefecture were observed and collected in February 2021 and March 2023; examination of herbarium specimens also revealed its occurrence in some other counties of Honghe Prefecture. Morphological observations were based on living plants in field and specimens deposited at IBSC and KUN. Measurements were taken with a ruler or stereomicroscope (EZ4W). The new species was compared with type specimens of similar species of Maesa available at the JSTOR Global Plants, as well as the specimens in BKF, E, HN, K and PE. Relevant taxonomic literature (Utteridge 2000, 2001, 2015, 2021; Utteridge and Saunders 2001, 2004; Sumanon et al. 2021, 2023) was extensively consulted. Morphological terminology follows Beentje (2016), Hewson (2019), Hickey (1979) and the Systematics Association Committee for Descriptive Biological Terminology (1962). The conservation status of the new species was assessed following the guidelines for using the IUCN Red List Categories and Criteria (IUCN Standards and Petitions Committee 2024).

Taxonomic treatment

Maesa flabellifera D.Wei, G.Hao & Utteridge, sp. nov.

Figs 1, 2

Type

China • Yunnan Province: Honghe Prefecture, Pingbian County, Dawei Mountain National Nature Reserve; 22.93, 103.69; 1871 m alt.; 26 February 2021 (fl.); D. Wei et al. Xu210531 (Holotype: IBSC! barcode IBSC1025516).

Diagnosis

Maesa flabellifera is morphologically similar to M. permollis, but clearly differs from the latter in the indumentum (lacking hairs vs. rusty hirsute hairs present), inflorescence structure (panicles 4.0−6.5 cm long with 7−16 branches vs. racemes or panicles 1−3 cm long with up to 3 branches). It is also similar to M. kurzii, but can be distinguished by the indumentum (lacking hairs vs. presence of rusty tomentose and strigose hairs) and lamina texture (membranaceous vs. chartaceous).

Figure 1. 

Holotype of Maesa flabellifera D.Wei, G.Hao & Utteridge, sp. nov. (D. Wei et al. Xu210531, IBSC1025516, IBSC).

Description

Large shrub, up to 2.5 m tall. Indumentum all parts lacking hairs, scales present on leaves, inflorescences and fruits, scales peltate, black, ± sessile, circular with irregular margins. Branches dark green with scattered lenticels, sparsely scaly. Leaves lamina broadly elliptic to obovate, 15−35 cm long, 6−20 cm wide, membranaceous, dark green above, pale grey-green below, adaxial and abaxial surface sparsely scaly; base obtuse to cuneate; margins serrulate-serrate with 20−34 teeth on each side; apex acuminate to obtuse, sometimes emarginate; mid-rib sparsely scaly adaxially and abaxially; secondary veins 10−18 pairs, craspedodromous; densely longitudinally glandular lines; petiole 1.5−3.0 cm long, sparsely scaly. Staminate inflorescences lateral (axillary), sometimes terminal, panicles, with 7−16 branches, 4.0−6.5 cm long, axis scaly; pedicels 0.5−1.5 mm long; bracts ovate, 1.20−1.65 mm long, scaly to densely scaly, margins entire, apex acute; bracteoles ± opposite, inserted at the base of the hypanthium, triangular, 0.90−1.35 mm long, 0.4−0.6 mm wide, apex acute, margins entire, scaly. Staminate flowers pentamerous, white; calyx lobes triangular, 1.25−1.60 mm long, 0.70−1.05 mm wide, margins entire, apex acute to rounded; corolla tube 1.9−2.3 mm long, corolla lobes broadly triangular, 1.45−1.55 mm long, 1.5−1.8 mm wide, margins entire, apex rounded; stamens 5, arising 0.8−1.0 mm from the base of the corolla, filaments 1.14−1.37 mm long, anthers 0.59−0.69 mm long; hypanthium 0.75−1.20 mm long, scaly to sparsely scaly; style 1.5−2.0 mm long, stigma ± 3-lobed. Pistillate inflorescences and flowers not seen. Fruits sub-globose, ca. 3.5 mm long, ca. 3 mm in diameter, scaly to sparsely scaly; pedicels at fruiting 0.50−1.66 mm long; bracteoles remaining ± opposite at the base of the fruit; persistent calyx lobes non-overlapping.

Figure 2. 

Maesa flabellifera A habitat B habit C node with petiole and base of inflorescence D abaxial and adaxial surfaces of leaf E inflorescence F bract (borne at base of pedicel) and bracteole (borne at base of the hypanthium) G flower after removal of corolla H corolla from G, opened flat I Infructescences.

Distribution and habitat

According to the specimens examined and the recent field investigations, Maesa flabellifera is presently found in Honghe Prefecture, Yunnan Province (Map 1). It is common in evergreen broad-leaved mixed forests at elevations of 1500−2200 m.

Phenology

Flowering from January to March, fruiting from April to December.

Etymology

The specific epithet ‘flabellifera’ is derived from the Latin ‘flabella’ and ‘fera’ to refer to its inflorescence with 7−16 branches of almost equal length and spreading, looking like a branching fan.

Vernacular name

Chinese Mandarin: shan xing du jing shan (扇形杜茎山).

Preliminary conservation status

Maesa flabellifera is widely distributed in southeast Yunnan. In the populations in the Dawei Mountain National Nature Reserves (43993 hm2) and Huanglian Mountain National Nature Reserves (65058 hm2), the habitats are well-protected and not threatened and individuals have been found locally common in each site. Based on currently available data, M. flabellifera is preliminarily assessed as Least Concern (LC) according to IUCN Categories and Criteria (IUCN Standards and Petitions Committee 2024).

Additional specimens examined (paratypes)

China, Yunnan, Honghe Prefecture • Yuanyang County, Xinjie Town; 1891 m alt.; 22 March 2023 (fl.); Wei et al. Xu231213 (IBSC, barcode IBSC1025520) • Lüchun County, Huanglian Mountain National Nature Reserve; 1865 m alt.; 23 March 2023 (fl.); Wei et al. Xu231222 (IBSC, barcode IBSC1025523) • Jinping County; 2192 m alt.; 16 January 2010 (fl.); Southeast Yunnan expedition. GBOWS956 (KUN, barcode KUN1279679) • Pingbian County; 1520 m alt.; 23 November 2009 (fr.); Qian et al. Pbdws151 (KUN, barcode KUN1339632).

Notes

Based on a phylogenetic analysis of molecular data, a new infrageneric classification of Maesa was proposed, dividing it into five subgenera, based on distribution and morphological characters (Sumanon et al. 2023). The species-level tree shows a strong signal of geographical distribution for the new infrageneric classification. It is speculated that Maesa flabellifera should be placed in the Maesa subg. Indicae Sumanon, Eiserhardt & Utteridge, by far the most species-rich subgenus in China, with species of trees or shrubs mainly from the Asian Continent, since its morphology and distribution is consistent with this clade especially the leaf morphology, such as the serrulate-serrate margins.

Map 1. 

Geographical distribution of Maesa flabellifera.

Maesa flabellifera belongs to the group of species with a longer corolla-tube. In the Flora Reipublicae Popularis Sinicae (Chen 1979), Maesa was divided into two sections based on the ratio of corolla-tube length to lobe length, namely Maesa sect. Maesa and M. sect. Doraena [Thunb.] Nakai. There are eight species with a long corolla-tube similar to M. flabellifera in sect. Doraena [Thunb.] Nakai. This treatment was not adopted in the Flora of China (Chen and Pipoly 1996). Although the long corolla-tube is a good character for species-level identification as a ‘spot character’, the group is not monophyletic in the phylogenetic analysis (Sumanon et al. 2023) and is used here as a comparative tool.

Maesa flabellifera is unique within the long corolla-tube species group, differing from all others by the following characters: lacking hairs on all parts; leaves thick, membranaceous and broadly elliptic to obovate, 15−35 cm long and 8−20 cm wide; long paniculate inflorescences, up to 6.5 cm long, with 7−16 branches, each branch almost equal in length, looking like a branching fan arising from the leaf axils.

In the key to Maesa in the Flora of China (Chen and Pipoly 1996), M. flabellifera would key out close to M. permollis Kurz as they share the same leaf features and the long corolla-tube. However, M. flabellifera is unlikely to be confused with M. permollis by examination of the indumentum and inflorescence structure. Based on the herbarium and field observations, M. permollis is conspicuously hairy throughout with rusty hirsute hairs and the inflorescences are short, dense clustering of numerous flowers, forming compact, many-flowered inflorescence clusters. Moreover, M. flabellifera is found in higher elevations around 1500−2200 m, compared to M. permollis which is encountered at lower elevations around 500−1600 m.

Compared to the other Maesa species with long corolla-tubes, M. flabellifera is most similar to M. kurzii, sharing broadly elliptic to obovate leaves and long paniculate inflorescences. However, the indumentum and lamina texture make M. flabellifera very distinctive and easily separated from M. kurzii, which has chartaceous leaves, usually rusty tomentose hairs throughout and inflorescences with rusty strigose hairs. Furthermore, the distributions of these two species are distinctly different and non-overlapping. Maesa flabellifera is currently only known from southeast Yunnan, situated in Honghe Prefecture. Maesa kurzii is located within Myanmar. A detailed comparison of these three species is shown in Table 1.

Table 1.

Morphological and ecological comparison between Maesa flabellifera and its allies.

Features M. flabellifera M. permollis M. kurzii
Indumentum lacking hairs rusty hirsute hairs rusty tomentose and strigose hairs
Leaf texture membranaceous membranaceous chartaceous
Inflorescence structure panicles with 7−16 branches racemes or panicles with up to 3 branches panicles with 4−10 branches
Inflorescence length 4.0−6.5 cm 1−3 cm 3.0−4.5 cm
Elevation 1500−2200 m 500−1600 m 500−1000 m

Acknowledgements

We greatly appreciate Herbaria of IBSC, KUN, BKF, E, HN, K and PE for access to specimen consultancy.

Additional information

Conflict of interest

The authors have declared that no competing interests exist.

Ethical statement

No ethical statement was reported.

Funding

The study was financially supported by the National Natural Science Foundation of China (grants no. 32070220 and 32070230).

Author contributions

All authors have contributed equally.

Author ORCIDs

Timothy M. A. Utteridge https://orcid.org/0000-0003-2823-0337

Data availability

All of the data that support the findings of this study are available in the main text.

References

  • Anderberg AA, Stähl B (1995) Phylogenetic interrelationships in the order Primulales, with special emphasis on the family circumscriptions. Canadian Journal of Botany 73(11): 1699–1730. https://doi.org/10.1139/b95-184
  • Anderberg AA, Stahl B, Källersjö M (1998) Phylogenetic relationships in the Primulales inferred from rbcL sequence data. Plant Systematics and Evolution 211: 93−102. https://doi.org/10.1007/BF00984914
  • APG [Angiosperm Phylogeny Group] (2016) An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV. Botanical Journal of Linnean Society 181(1): 1–20. https://doi.org/10.1111/boj.12385
  • Beentje H (2016) The Kew Plant Glossary: an illustrated dictionary of plant terms, second edition. Royal Botanic Gardens Kew, London, 192.
  • Bremer B, Bremer K, Chase MW, Fay MF, Reveal JL, Bailey LH, Soltis DE, Soltis PS, Stevens PF (2009) An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III. Botanical Journal of Linnean Society 161(2): 105−121. https://doi.org/10.1111/j.1095-8339.2009.00996.x
  • Chen J (1979) Myrsinaceae. In: Chen J (Ed.) Flora Reipublicae Popularis Sinicae 58. Science Press, Beijing, 1−38.
  • Chen J, Pipoly JJ (1996) Myrsinaceae. In: Wu ZY, Raven PH (Eds) Flora of China 15. Science Press, Beijing and Missouri Botanical Garden Press, St Louis, 1–38.
  • Ding HB, Wang LY, Quan DL, Yang B, Yue MM, Wang PY, Yang YJW, Gong QB, Zhou SS, Wang L, Li JW, Tan YH (2023) Additions to the seed plant flora in Yunnan, China. Biodiversity Science 31(10): 23254, 1–12. https://doi.org/10.17520/biods.2023254
  • Hewson HJ (2019) Plant Indumentum: A Handbook of Terminology, Revised edition. Australian Biological Resources Study, Commonwealth Department of the Environment and Energy, 47 pp.
  • Hickey LJ (1979) A revised classification of the architecture of dicotyledonous leaves. In: Metcalfe CR, Chalk L (Eds) Anatomy of the Dicotyledon. Clarendon Press, Oxford, 25−39.
  • IUCN Standards and Petitions Committee (2024) Guidelines for using the IUCN Red List categories and criteria. Version 16: Prepared by the Standards and Petitions Committee in March 2024.
  • Källersjö M, Bergqvist G, Anderberg AA (2000) Generic realignment in primuloid families of the Ericales s.l.: a phylogenetic analysis based on DNA sequences from three chloroplast genes and morphology. American Journal Botany 87(9): 1325–1341. https://doi.org/10.2307/2656725
  • Mez C (1902) Myrsinaceae. In: Engler A (Ed.) Das Pflanzenreich 9. IV.236. Wilhelm Engelmann, Berlin, 1–437.
  • Sumanon P, Balslev H, Utteridge TMA, Eiserhardt WL (2023) A species-level phylogenetic framework and infrageneric classification for the genus Maesa (Primulaceae). Taxon 72(4): 1–20. https://doi.org/10.1002/tax.12991
  • Systematics Association Committee for Descriptive Biological Terminology (1962) IIa. Terminology of Simple Symmetrical Plane Shapes (Chart 1a), Addendum. Taxon 11(8): 245–247. https://doi.org/10.2307/1217034
  • Utteridge TMA (2000) Two new species of Maesa (Myrsinaceae) from Puncak Jaya, New Guinea. Contributions to the Flora of Mt. Jaya, I. Kew Bulletin 55: 443–449. https://doi.org/10.2307/4115658
  • Utteridge TMA (2021) Flora of Singapore precursors 26: The genus Maesa (Primulaceae) in Singapore and clarification of Maesa ramentacea in Malesia. Gardens’ Bulletin Singapore 73(2): 267–278. https://doi.org/10.26492/gbs73(2).2021-04
  • Walker EH (1940) A revision of the eastern Asiatic Myrsinaceae. Philippine Journal of Sciences 73(1/2): 1−258.
  • Yu SX, Hao G, Jin XF (2016) Spermatophytes. In: Chen YY (Ed.) Species Catalogue of China 1. VII. Science Press, Beijing, 128–130.
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